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Pyrrolidine, 1-[[(phenylmethyl)amino]acetyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

102179-28-2

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102179-28-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102179-28-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,1,7 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 102179-28:
(8*1)+(7*0)+(6*2)+(5*1)+(4*7)+(3*9)+(2*2)+(1*8)=92
92 % 10 = 2
So 102179-28-2 is a valid CAS Registry Number.

102179-28-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Pyrrolidinocarbonylmethyl-benzylamin

1.2 Other means of identification

Product number -
Other names 2-Benzylamino-1-pyrrolidin-1-yl-ethanone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:102179-28-2 SDS

102179-28-2Downstream Products

102179-28-2Relevant academic research and scientific papers

Fluoro-olefins as peptidomimetic inhibitors of dipeptidyl peptidases

Van Der Veken, Pieter,Senten, Kristel,Kertèsz, István,De Meester, Ingrid,Lambeir, Anne-Marie,Maes, Marie-Berthe,Scharpé, Simon,Haemers, Achiel,Augustyns, Koen

, p. 1768 - 1780 (2007/10/03)

The feasibility of the fluoro-olefin function as a peptidomimetic group in inhibitors for dipeptidyl peptidase IV and II (DPP IV and DPP II) is investigated by evaluation of N-substituted Gly-Ψ[CF=C]pyrrolidines, Gly-Ψ[CF=C]piperidines, and Gly-Ψ[CF=C](2-cyano)pyrrolidines. Of this later class, the (Z)- and (E)-fluoro-olefin analogues were prepared and chemical stability in comparison with the parent amide was checked. Most of these compounds exhibited a strong binding preference toward DPP II with IC 50 values in the low micromolar range, while only low DPP IV inhibitory potential is seen.

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